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Number of items: 13.

Niarchou, Maria, Calkins, Monica E., Moore, Tyler M., Tang, Sunny, X., McDonald-McGinn, Donna M., Zackai, Elaine H., Emanuel, Beverly S., Gur, Ruben C. and Gur, Raquel E. 2017. Attention deficit hyperactivity disorder symptoms and psychosis in 22q11.2 deletion syndrome. Schizophrenia Bulletin
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Chawner, Samuel, Doherty, Joanne L., Moss, Hayley, Niarchou, Maria, Walters, James, Owen, Michael J. and Van Den Bree, Marianne Bernadette 2017. Childhood cognitive development in 22q11.2 deletion syndrome: case–control study. British Journal of Psychiatry 211 (4) , pp. 223-230. 10.1192/bjp.bp.116.195651

Gur, RE, Bassett, AS, McDonald-McGinn, DM, Bearden, CE, Chow, E, Emanuel, BS, Owen, M, Swillen, A, Van Den Bree, Marianne Bernadette, Vermeesch, J, Vorstman, JAS, Warren, S, Lehner, T, Morrow, B and Niarchou, Maria 2017. A neurogenetic model for the study of schizophrenia spectrum disorders: The International 22q11.2 Deletion Syndrome Brain Behavior Consortium. Molecular Psychiatry 22 , pp. 1664-1672.

Niarchou, Maria, Moore, Tyler M., Tang, Sunny X., Calkins, Monica E., McDonald-McGuinn, Donna M., Zackai, Elaine H., Emanuel, Beverly S., Gur, Ruben C. and Gur, Raquel E. 2017. The dimensional structure of psychopathology in 22q11.2 Deletion Syndrome. Journal of Psychiatric Research 92 , pp. 124-131. 10.1016/j.jpsychires.2017.04.006

Niarchou, Maria, Martin, Joanna, Thapar, Anita, Owen, Michael John and van den Bree, Marianne Bernadette 2015. The clinical presentation of attention deficit-hyperactivity disorder (ADHD) in children with 22q11.2 deletion syndrome. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 168 (8) , pp. 730-738. 10.1002/ajmg.b.32378

Niarchou, Maria, Zammit, Stanley and Lewis, Glyn 2015. The Avon Longitudinal Study of Parents and Children (ALSPAC) birth cohort as a resource for studying psychopathology in childhood and adolescence: a summary of findings for depression and psychosis. Social Psychiatry and Psychiatric Epidemiology 50 (7) , pp. 1017-1027. 10.1007/s00127-015-1072-8

Niarchou, Maria, Zammit, Stanley, Escott-Price, Valentina, Owen, Michael John and van den Bree, Marianne Bernadette 2014. Exploring the indirect effects of catechol-O-methyltransferase (COMT) genotype on psychotic experiences through cognitive function and anxiety disorders in a large birth cohort of children. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 165 (5) , pp. 410-420. 10.1002/ajmg.b.32245

Schneider, Maude, Debbané, Martin, Bassett, Anne S., Chow, Eva W.C., Fung, Wai Lun Alan, van den Bree, Marianne Bernadette, Owen, Michael John, Murphy, Kieran C., Niarchou, Maria, Kates, Wendy R., Antshel, Kevin M., Fremont, Wanda, McDonald-McGinn, Donna M., Gur, Raquel E., Zackai, Elaine H., Vorstman, Jacob, Duijff, Sasja N., Klaassen, Petra W.J., Swillen, Ann, Gothelf, Doron, Green, Tamar, Weizman, Abraham, Van Amelsvoort, Therese, Evers, Laurens, Boot, Erik, Shashi, Vandana, Hooper, Stephen R., Bearden, Carrie E., Jalbrzikowski, Maria, Armando, Marco, Vicari, Stefano, Murphy, Declan G., Ousley, Opal, Campbell, Linda E., Simon, Tony J. and Eliez, Stephan 2014. Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: Results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. American Journal of Psychiatry 171 (6) , pp. 627-639. 10.1176/appi.ajp.2013.13070864

Monks, Stephen, Niarchou, Maria, Davies, Aimee, Walters, James Tynan Rhys, Williams, Nigel Melville, Owen, Michael John, van den Bree, Marianne Bernadette and Murphy, Kieran 2014. Further evidence for high rates of schizophrenia in 22q11.2 deletion syndrome. Schizophrenia Research 153 (1-3) , pp. 231-236. 10.1016/j.schres.2014.01.020

Niarchou, Maria, Zammit, Stanley, van Goozen, Stephanie Helena Maria, Thapar, Anita, Tierling, Hayley, Owen, Michael John and van den Bree, Marianne Bernadette 2014. Psychopathology and cognition in children with 22q11.2 deletion syndrome. British Journal of Psychiatry 204 (1) , pp. 46-54. 10.1192/bjp.bp.113.132324

Niarchou, Maria, Zammit, Stanley, Walters, James Tynan Rhys, Lewis, Glyn, Owen, Michael John and van den Bree, Marianne Bernadette 2013. Defective processing speed and nonclinical psychotic experiences in children: longitudinal analyses in a large birth cohort. American Journal of Psychiatry 170 (5) , pp. 550-557. 10.1176/appi.ajp.2012.12060792

Delio, Maria, Guo, Tingwei, McDonald-McGinn, Donna M., Zackai, Elaine, Herman, Sean, Kaminetzky, Mark, Higgins, Anne Marie, Coleman, Karlene, Chow, Carolyn, Jarlbrzkowski, Maria, Bearden, Carrie E., Bailey, Alice, Vangkilde, Anders, Olsen, Line, Olesen, Charlotte, Skovby, Flemming, Werge, Thomas M., Templin, Ludivine, Busa, Tiffany, Philip, Nicole, Swillen, Ann, Vermeesch, Joris R., Devriendt, Koen, Schneider, Maude, Dahoun, Sophie, Eliez, Stephan, Schoch, Kelly, Hooper, Stephen R., Shashi, Vandana, Samanich, Joy, Marion, Robert, van Amelsvoort, Therese, Boot, Erik, Klaassen, Petra, Duijff, Sasja N., Vorstman, Jacob, Yuen, Tracy, Silversides, Candice, Chow, Eva, Bassett, Anne, Frisch, Amos, Weizman, Abraham, Gothelf, Doron, Niarchou, Maria, van den Bree, Marianne Bernadette, Owen, Michael John, Suñer, Damian Heine, Andreo, Jordi Rosell, Armando, Marco, Vicari, Stefano, Digilio, Maria Cristina, Auton, Adam, Kates, Wendy R., Wang, Tao, Shprintzen, Robert J., Emanuel, Beverly S. and Morrow, Bernice E. 2013. Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes. American Journal of Human Genetics 92 (3) , pp. 439-447. 10.1016/j.ajhg.2013.01.018

Niarchou, Maria 2013. Cognition, psychopathology and the role of genetic variation in Catechol-O-Methyltransferase in children at increased risk of schizophrenia. PhD Thesis, Cardiff University.
Item availability restricted.

This list was generated on Sun Apr 22 03:14:44 2018 BST.